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Nicorette
Nicorette - 0135-0532-08 - (nicotine polacrilex)
Drug Information of Nicorette
| Product NDC: | 0135-0532 |
| Proprietary Name: | Nicorette |
| Non Proprietary Name: | nicotine polacrilex |
| Active Ingredient(s): | 2 mg/1 & nbsp; nicotine polacrilex |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GUM, CHEWING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nicorette
| Product NDC: | 0135-0532 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA018612 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20111115 |
Package Information of Nicorette
| Package NDC: | 0135-0532-08 |
| Package Description: | 20 GUM, CHEWING in 1 CARTON (0135-0532-08) |
NDC Information of Nicorette
| NDC Code | 0135-0532-08 |
| Proprietary Name | Nicorette |
| Package Description | 20 GUM, CHEWING in 1 CARTON (0135-0532-08) |
| Product NDC | 0135-0532 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | nicotine polacrilex |
| Dosage Form Name | GUM, CHEWING |
| Route Name | ORAL |
| Start Marketing Date | 20111115 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | NICOTINE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
